Tag | Content |
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EnhancerAtlas ID | HS064-07265 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr19:7185490-7186830 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr19:7185903-7185921 | GGAAGGAAGGAAAAAAAA | + | 6.18 | EWSR1-FLI1 | MA0149.1 | chr19:7185895-7185913 | AAAAGGAAGGAAGGAAGG | + | 7.95 | EWSR1-FLI1 | MA0149.1 | chr19:7185899-7185917 | GGAAGGAAGGAAGGAAAA | + | 9.07 | IRF1 | MA0050.2 | chr19:7186206-7186227 | AAACAAAAAATGAAACAAAAC | - | 6.78 | IRF1 | MA0050.2 | chr19:7186690-7186711 | TTTTACTTTCTTTTTCTTTTC | + | 7.71 | IRF9 | MA0653.1 | chr19:7186620-7186635 | AACCAAACTGAAACT | + | 6.61 | POU2F2 | MA0507.1 | chr19:7185559-7185572 | ACATGCAAATGTG | - | 6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I007185 | chr19 | 7185868 | 7187067 |
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Enhancer Sequence | AAAAAAGTGG CTGCAGATCC TGCCTTTGGG AGCACAAGGT CTAATGGAGG AGACATGTTA 60 GTTACTTAAA CATGCAAATG TGGCTCGGTG TGGTGGCTCA CGCCTGTAAT CCTAGCAATT 120 TGGGAGGTCG AGGCGGGTGG ATCACCTGAG GTCAGGAGTT TGAGACCAGC CTGGTCAACA 180 TGGTGAAACC CTGTCTCTAC TAAAAATACA AAAATTAGCT AGGTGTGCTG GTGCATGCCT 240 GTAATCCCAG CTGCTCAGGA GGCTGAGGCA CGAGAATCAC TTGAATCTGG GAGGTGGAGG 300 CTGCAGTGAG CCATGATCGT GCCACTATAC TCCAGCCTGG GCAACAAGTG CAAAATTCTG 360 TCAAAAAAAA AAAAAAAAAA GAGAGAGAGA GACAAAGAGA GAGAGAAAAG GAAGGAAGGA 420 AGGAAAAAAA AAAGGCTGGT TGTGGTGGCT CATGCCTGTA ATCCTAGCAC TTTGGGAGGC 480 CAAGGTGGGC GGATCACCTG AGGTCAGGAG TTTCAGACCA GCCTGGCCAA CATGGTGAAA 540 CCCCATCTCT ACTGATGATA CAAACAATTA GCCGGGTGTG GTGGTGGGCG TCTGTAATCC 600 CAGCTACTCA GGAGGCTGAG GCAGGAGAAT CGCTTGAACC TGGGAGGGGA GGTTGCAGGG 660 AGCCGAGATC ATGCCACTGC ACTCCAGCCT TGGTGACAGA GGGAGACTCT GTCTCAAAAC 720 AAAAAATGAA ACAAAACAAA AAATAAGAAA GAAAGTTGGG GAGTGTTCTT CACCCCAAAT 780 CCCCAGACTG TGATTCTCAG CACAGTGGAT CCCACCGGCC AAACTCAGGG AACAGAAGTG 840 GCCCCAGAAG CTACATCCAT ATATGAACAG CACCATCTGG TCGAAATTTC TGCGATGACG 900 GAAATGTTCT CTATCTGGGC CATCCAACAT AGTAGCCACT TCTCCCCTGT GGCTTCTGAA 960 TGTGCTTAGT GCAACTAGGA AATCCAATTT TTTTTTTAAT TGTGGTAAAA TACACATAGC 1020 ATAAAATTCA CCATTGTAAT CATGTTTAAA TGTATAGTTC AGTGGTATTA AATACTTTTA 1080 TGTGGCTATG CAACCATCAC CACCACCCAT CTCCAGAACT TTCTCACCTT AACCAAACTG 1140 AAACTCTGCC CCCATGAAAC AGTCACACTC ATCCTCCTCC CCAACTCCTG GCACCTGCCA 1200 TTTTACTTTC TTTTTCTTTT CTTTTTTTTT ATTTTTATTT TTTGAGATGG AGTCTTGCTT 1260 TGTTGCCCAG GCTGGGGTGC AGTGGCGCGA TCTCAGCTCA CTGTAACCTC TGCCTCCCGG 1320 GTTCAAGTGA TTCTCCTGCC 1340
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